Transcriptional mechanisms and protein kinase signaling mediate organic dust induction of IL-8 expression in lung epithelial and THP-1 cells

Am J Physiol Lung Cell Mol Physiol. 2015 Jan 1;308(1):L11-21. doi: 10.1152/ajplung.00215.2014. Epub 2014 Nov 14.

Abstract

Exposure to the agricultural work environment is a risk factor for the development of respiratory symptoms and chronic lung diseases. Inflammation is an important contributor to the pathogenesis of tissue injury and disease. Cellular and molecular mechanisms mediating lung inflammatory responses to agricultural dust are not yet fully understood. We studied the effects of poultry dust extract on molecular regulation of interleukin-8 (IL-8), a proinflammatory cytokine, in A549 and Beas2B lung epithelial and THP-1 monocytic cells. Our findings indicate that poultry dust extract potently induces IL-8 levels by increasing IL-8 gene transcription without altering IL-8 mRNA stability. Increase in IL-8 promoter activity was due to enhanced binding of activator protein 1 and NF-κB. IL-8 induction was associated with protein kinase C (PKC) and mitogen-activated protein kinase (MAPK) activation and inhibited by PKC and MAPK inhibitors. IL-8 increase was not inhibited by polymyxin B or l-nitroarginine methyl ester, indicating lack of involvement of lipopolysaccharide and nitric oxide in the induction. Lung epithelial and THP-1 cells share common mechanisms for induction of IL-8 levels. Our findings identify key roles for transcriptional mechanisms and protein kinase signaling pathways for IL-8 induction and provide insights into the mechanisms regulating lung inflammatory responses to organic dust exposure.

Keywords: chemokine; lipopolysaccharide; lung inflammation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cell Line, Tumor
  • Dust*
  • Epithelial Cells / metabolism*
  • Epithelial Cells / pathology
  • Gene Expression Regulation / drug effects*
  • Humans
  • Interleukin-8 / biosynthesis*
  • MAP Kinase Signaling System / drug effects*
  • Monocytes / metabolism*
  • Monocytes / pathology
  • Protein Kinase Inhibitors / pharmacology
  • Respiratory Mucosa / metabolism*
  • Respiratory Mucosa / pathology
  • Transcription, Genetic / drug effects*

Substances

  • CXCL8 protein, human
  • Dust
  • Interleukin-8
  • Protein Kinase Inhibitors